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Cryopreservation of Human Mucosal Leukocytes.
Hughes, Sean M; Shu, Zhiquan; Levy, Claire N; Ferre, April L; Hartig, Heather; Fang, Cifeng; Lentz, Gretchen; Fialkow, Michael; Kirby, Anna C; Adams Waldorf, Kristina M; Veazey, Ronald S; Germann, Anja; von Briesen, Hagen; McElrath, M Juliana; Dezzutti, Charlene S; Sinclair, Elizabeth; Baker, Chris A R; Shacklett, Barbara L; Gao, Dayong; Hladik, Florian.
Afiliação
  • Hughes SM; Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, United States of America.
  • Shu Z; Department of Mechanical Engineering, University of Washington, Seattle, Washington, United States of America.
  • Levy CN; School of Mechanical and Materials Engineering, Washington State University, Everett, Washington, United States of America.
  • Ferre AL; Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, United States of America.
  • Hartig H; Department of Medical Microbiology and Immunology, School of Medicine, University of California Davis, Davis, California, United States of America.
  • Fang C; Department of Medicine, University of California San Francisco, San Francisco, California, United States of America.
  • Lentz G; Department of Mechanical Engineering, University of Washington, Seattle, Washington, United States of America.
  • Fialkow M; Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, United States of America.
  • Kirby AC; Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, United States of America.
  • Adams Waldorf KM; Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, United States of America.
  • Veazey RS; Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington, United States of America.
  • Germann A; Division of Comparative Pathology, Tulane National Primate Research Center, Tulane University School of Medicine, Covington, Louisiana, United States of America.
  • von Briesen H; Division of Medical Biotechnology, Fraunhofer Institute for Biomedical Engineering IBMT, Sulzbach/Saar, Germany.
  • McElrath MJ; Division of Medical Biotechnology, Fraunhofer Institute for Biomedical Engineering IBMT, Sulzbach/Saar, Germany.
  • Dezzutti CS; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
  • Sinclair E; Department of Medicine, University of Washington, Seattle, Washington, United States of America.
  • Baker CA; Department of Laboratory Medicine, University of Washington, Seattle, Washington, United States of America.
  • Shacklett BL; Department of Global Health, University of Washington, Seattle, Washington, United States of America.
  • Gao D; School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
  • Hladik F; Magee-Womens Research Institute, Pittsburgh, Pennsylvania, United States of America.
PLoS One ; 11(5): e0156293, 2016.
Article em En | MEDLINE | ID: mdl-27232996
ABSTRACT

BACKGROUND:

Understanding how leukocytes in the cervicovaginal and colorectal mucosae respond to pathogens, and how medical interventions affect these responses, is important for developing better tools to prevent HIV and other sexually transmitted infections. An effective cryopreservation protocol for these cells following their isolation will make studying them more feasible. METHODS AND

FINDINGS:

To find an optimal cryopreservation protocol for mucosal mononuclear leukocytes, we compared cryopreservation media and procedures using human vaginal leukocytes and confirmed our results with endocervical and colorectal leukocytes. Specifically, we measured the recovery of viable vaginal T cells and macrophages after cryopreservation with different cryopreservation media and handling procedures. We found several cryopreservation media that led to recoveries above 75%. Limiting the number and volume of washes increased the fraction of cells recovered by 10-15%, possibly due to the small cell numbers in mucosal samples. We confirmed that our cryopreservation protocol also works well for both endocervical and colorectal leukocytes. Cryopreserved leukocytes had slightly increased cytokine responses to antigenic stimulation relative to the same cells tested fresh. Additionally, we tested whether it is better to cryopreserve endocervical cells on the cytobrush or in suspension.

CONCLUSIONS:

Leukocytes from cervicovaginal and colorectal tissues can be cryopreserved with good recovery of functional, viable cells using several different cryopreservation media. The number and volume of washes has an experimentally meaningful effect on the percentage of cells recovered. We provide a detailed, step-by-step protocol with best practices for cryopreservation of mucosal leukocytes.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Criopreservação / Leucócitos / Mucosa Tipo de estudo: Guideline Limite: Female / Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Criopreservação / Leucócitos / Mucosa Tipo de estudo: Guideline Limite: Female / Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos